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Published in 2020 at "Frontiers in Neuroscience"
DOI: 10.3389/fnins.2020.00749
Abstract: Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a progressive autosomal dominantly inherited cerebellar ataxia characterized by the aggregation of polyglutamine-expanded protein within neuronal nuclei in the brain, which can lead to brain damage that precedes…
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Keywords:
imaging sca3;
sca3 mjd;
brain;
magnetic resonance ... See more keywords